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DESIGN AND APPLICATION OF
  DIGITAL MICRO FLUIDIC
         BIOCHIP
         Presented by :




  BENGAL INSTITUTE OF TECHNOLOGY
•   What is biochip?
•   Types of Biochip
•   Introduction
•   Motivation for Biochip
•   Digital Microfluidic Biochip
•   Actuation Principle
•   Advantages
•   Application
•   Conclusion
Biosensor or bioprocessor that utilizes
technologies of modern Biology and
Electronics in a micro scale.
 DNA chip
 Protein chip
 Enzyme chip
 Lab-on-a-chip
 Lab-on-chip:
    Systems for performing biomedical analyses
     of very small quantities of liquids
 Advantages:
    Fast reaction times
    Low-cost, portable and disposable
    Compactness massive parallelization
     high-throughput
 Types:
    Continuous-flow:
     enclosed, interconnecting, micron-dimension
     channels
    Digital: discrete droplets of fluid across the
     surface of an array of electrodes.
Classification of Biochip
 Transfer conventional biochemical
  laboratory methods to lab-on-a-chip
  (LoC), or microfluidic biochips

 Potential to revolutionize biosensing,
  clinical diagnostics, drug discovery
        -Small size and sample volumes
        -Lower cost
        -Higher sensitivity
 Based on precise control of very small volumes
  of liquids
 Integrate various fluid-handling functions such as
  sample preparation, analysis, separation, and
  detection
 Most commercially available microfluidic devices are
  continuous-flow
   -Permanently etched microchannels, pumps, and
   valves




                  (Duke University)
                        2002
 Digital microfluidic biochips (DMBs)
    -Manipulate discrete droplets (smaller volumes)
    -Electrical actuation
    -No need for cumbersome micropumps and
    microvalves
    -Dynamic reconfigurability (virtual routes)
    -Architectural scalability and greater automation




   Fig. 2. (a) Basic cell used in an EWOD-based digital micro
   fluidic biochip; (b) a two-dimensional array for digital
   micro fluidics [Pollack 2001].
 Droplets containing samples
  travel inside filler medium
  (e.g., silicone oil), sandwiched in
  between glass plates
 Bottom plate – patterned array
  of control electrodes
 Top plate – continuous ground
  electrode
 Surfaces are insulated (Parylene)
  and hydrophobic (Teflon AF)
 Droplet transport occurs by
  removing potential
  on current electrode, applying
  potential on an adjacent
  electrode
 Interfacial tension
  gradient created
Fig. 4. Side-view of digital micro fluidic platform with a conductive
glass top plate (left). Materials and construction of the actuator
(right). By adding a conductive top plate and adding individually
addressed buried electrodes in the bottom plate, the droplet can be
actuated from one electrode position to the next by the application of
voltage.
 It has no moving parts.
 It requires no channels.
 It controls many droplets independently because
  the electro wetting force is localized at the
  surface.
 It works with a wide variety of liquids ----- that is,
  most electrolytic solution.
 It is compatible with microscopy. Glass substrate
  and transparent indium-tin-oxide (ITO)
  electrodes makes the chip compatible with
  observation from a microscope.
 It is extremely energy efficient ---- using
  nanowatts to microwatts of power per transfer.
 In most diagnostic and chemical detection
   applications, a key challenge is the preparation of
   the analyzed for the presentation to the on-chip
   detection system.
 In tissue-engineering application, the challenge is
   to high-resolution (less than 10 micron) 3D tissue
   constructs with embedded cells and growth
   factors by manipulating and maintaining live cells
   on the chip platform.
 A new application can be introduced, including
  detection of airborne sulfates obtained by air
  sampling, DNA pyro sequencing, and a biomimetic
  manufacturing process for soft-tissue
  engineering.
 On-chip assays for determining the concentration
  of target analysts is a natural application for
  digital micro fluidics.
o This technique is faster for analyzing various
  components present in blood, urine, split as well
  as air born sample.
o Small amount of sample is enough to test various
  parameters.
o Small size instrument is also advantages upon
  conventional analyzer, which can easily carry and
  also goes in spacecraft for diagnosis.
o Cost effectiveness is also an important advantage
  over the conventional instrument.
o In a very short time various parameters can be
  tested simultaneously from a sample.
THANK YOU

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Biochip

  • 1. DESIGN AND APPLICATION OF DIGITAL MICRO FLUIDIC BIOCHIP Presented by : BENGAL INSTITUTE OF TECHNOLOGY
  • 2. What is biochip? • Types of Biochip • Introduction • Motivation for Biochip • Digital Microfluidic Biochip • Actuation Principle • Advantages • Application • Conclusion
  • 3. Biosensor or bioprocessor that utilizes technologies of modern Biology and Electronics in a micro scale.
  • 4.  DNA chip  Protein chip  Enzyme chip  Lab-on-a-chip
  • 5.  Lab-on-chip:  Systems for performing biomedical analyses of very small quantities of liquids  Advantages:  Fast reaction times  Low-cost, portable and disposable  Compactness massive parallelization high-throughput  Types:  Continuous-flow: enclosed, interconnecting, micron-dimension channels  Digital: discrete droplets of fluid across the surface of an array of electrodes.
  • 7.  Transfer conventional biochemical laboratory methods to lab-on-a-chip (LoC), or microfluidic biochips  Potential to revolutionize biosensing, clinical diagnostics, drug discovery -Small size and sample volumes -Lower cost -Higher sensitivity
  • 8.  Based on precise control of very small volumes of liquids  Integrate various fluid-handling functions such as sample preparation, analysis, separation, and detection  Most commercially available microfluidic devices are continuous-flow -Permanently etched microchannels, pumps, and valves (Duke University) 2002
  • 9.  Digital microfluidic biochips (DMBs) -Manipulate discrete droplets (smaller volumes) -Electrical actuation -No need for cumbersome micropumps and microvalves -Dynamic reconfigurability (virtual routes) -Architectural scalability and greater automation Fig. 2. (a) Basic cell used in an EWOD-based digital micro fluidic biochip; (b) a two-dimensional array for digital micro fluidics [Pollack 2001].
  • 10.  Droplets containing samples travel inside filler medium (e.g., silicone oil), sandwiched in between glass plates  Bottom plate – patterned array of control electrodes  Top plate – continuous ground electrode  Surfaces are insulated (Parylene) and hydrophobic (Teflon AF)  Droplet transport occurs by removing potential on current electrode, applying potential on an adjacent electrode  Interfacial tension gradient created
  • 11. Fig. 4. Side-view of digital micro fluidic platform with a conductive glass top plate (left). Materials and construction of the actuator (right). By adding a conductive top plate and adding individually addressed buried electrodes in the bottom plate, the droplet can be actuated from one electrode position to the next by the application of voltage.
  • 12.  It has no moving parts.  It requires no channels.  It controls many droplets independently because the electro wetting force is localized at the surface.  It works with a wide variety of liquids ----- that is, most electrolytic solution.  It is compatible with microscopy. Glass substrate and transparent indium-tin-oxide (ITO) electrodes makes the chip compatible with observation from a microscope.  It is extremely energy efficient ---- using nanowatts to microwatts of power per transfer.
  • 13.  In most diagnostic and chemical detection applications, a key challenge is the preparation of the analyzed for the presentation to the on-chip detection system.  In tissue-engineering application, the challenge is to high-resolution (less than 10 micron) 3D tissue constructs with embedded cells and growth factors by manipulating and maintaining live cells on the chip platform.  A new application can be introduced, including detection of airborne sulfates obtained by air sampling, DNA pyro sequencing, and a biomimetic manufacturing process for soft-tissue engineering.  On-chip assays for determining the concentration of target analysts is a natural application for digital micro fluidics.
  • 14. o This technique is faster for analyzing various components present in blood, urine, split as well as air born sample. o Small amount of sample is enough to test various parameters. o Small size instrument is also advantages upon conventional analyzer, which can easily carry and also goes in spacecraft for diagnosis. o Cost effectiveness is also an important advantage over the conventional instrument. o In a very short time various parameters can be tested simultaneously from a sample.